MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: inflammatory disease (MONDO:0021166)
Parent Node: inner ear disease (MONDO:0002467)
..Starting node ..labyrinthitis ()
Child Nodes:
........focal labyrinthitis ()
........infectious otitis interna ()
........purulent labyrinthitis ()
........serous labyrinthitis ()
........toxic labyrinthitis ()
........viral labyrinthitis ()
Sister Nodes:
..autoimmune inner ear disease ()
..cochlear disease ()
..enlarged vestibular aqueduct syndrome ()
..inner ear neoplasm ()
..labyrinthine dysfunction ()
..labyrinthitis ()
..motion sickness ()
..otosclerosis (disease) ()
..vestibular disease ()
..X-linked mixed deafness with perilymphatic gusher ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2008
Name:	labyrinthitis
Definition:	Inflammation of the inner ear. The cause is often not clear. It may be due to a virus, but it can also arise from bacterial infection, head injury, extreme stress, an allergy, or as a reaction to medication.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	inflammation of internal ear; inner ear infection; internal ear inflammation; otitis interna
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: AARS;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal